geneid | 4809 |
---|---|
ensemblid | ENSG00000100138.15 |
hgncid | 7819 |
symbol | SNU13 |
name | small nuclear ribonucleoprotein 13 |
refseq_nuc | NM_001003796.2 |
refseq_prot | NP_001003796.1 |
ensembl_nuc | ENST00000401959.6 |
ensembl_prot | ENSP00000383949.1 |
mane_status | MANE Select |
chr | chr22 |
start | 41673933 |
end | 41688867 |
strand | - |
ver | v1.2 |
region | chr22:41673933-41688867 |
region5000 | chr22:41668933-41693867 |
regionname0 | SNU13_chr22_41673933_41688867 |
regionname5000 | SNU13_chr22_41668933_41693867 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 128 | 376 | 88 | 72 | 154 | 16 | 44 | 116 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 387 | 359 | 83 | 68 | 147 | 16 | 43 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
c0002 | 0/0 | 387 | 17 | 5 | 4 | 7 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1072 | 208 | 68 | 24 | 97 | 5 | 13 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0002 | 0/0 | 1072 | 74 | 2 | 13 | 40 | 5 | 14 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0003 | 1/0 | 1072 | 68 | 2 | 30 | 17 | 3 | 15 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0004 | 0/0 | 1072 | 10 | 7 | 3 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0005 | 0/0 | 1072 | 6 | 6 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0006 | 0/0 | 1072 | 5 | 0 | 2 | 0 | 3 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0007 | 0/0 | 1072 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0008 | 0/0 | 1072 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0009 | 0/0 | 1072 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
t0010 | 0/0 | 1072 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 47 | 1 | 20 | 11 | 3 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0002 | 0/0 | 46 | 4 | 12 | 22 | 2 | 6 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0003 | 0/0 | 44 | 1 | 10 | 17 | 5 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0004 | 0/0 | 39 | 3 | 1 | 34 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0019 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 387 | 359 | 83 | 68 | 147 | 16 | 43 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0002 | 0/0 | 387 | 17 | 5 | 4 | 7 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1458 | 191 | 63 | 20 | 90 | 5 | 12 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0002 | 0/0 | 1458 | 74 | 2 | 13 | 40 | 5 | 14 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0003 | 1/0 | 1458 | 68 | 2 | 30 | 17 | 3 | 15 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0004 | 0/0 | 1458 | 10 | 7 | 3 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0005 | 0/0 | 1458 | 6 | 6 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0006 | 0/0 | 1458 | 5 | 0 | 2 | 0 | 3 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0007 | 0/0 | 1458 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0008 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0009 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0001t0010 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
a0001c0002t0001 | 0/0 | 1458 | 17 | 5 | 4 | 7 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | copy fasta | chr22 | 41668933 | 41693867 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 46 | 4 | 12 | 22 | 2 | 6 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0004 | 0/0 | 39 | 3 | 1 | 34 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0019 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0003 | 0/0 | 44 | 1 | 10 | 17 | 5 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0001 | 1/0 | 47 | 1 | 20 | 11 | 3 | 11 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0004g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0005g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0006g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0007g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0094 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0093 | EUR | IBS | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0040 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03492 | hp2 | a0001 | c0001 | t0007 | g0040 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0018 | EUR | TSI | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | GIH | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG02559 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | ACB | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0001 | REF | REF | SNU13_chr22_41668933_41693867 | SNU13 | chr22 | 41668933 | 41693867 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41680326
|
G | A | 1 | a0001c0002 | 17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
synonymous_variant | LOW | c.42C>T | p.Ala14Ala | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/3 | 113/1458 | 42/387 | 14/128 | chr22 | 41680326 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41673996
|
C | G | 2 | a0001c0001t0005a0001c0001t0010 | 7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 937 | chr22 | 41673996 | |||||
chr22:41674223
|
G | A | 1 | a0001c0001t0004 | 10 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*710C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 710 | chr22 | 41674223 | |||||
chr22:41674272
|
T | C | 9 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*661A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 661 | chr22 | 41674272 | |||||
chr22:41674313
|
G | A | 2 | a0001c0001t0005a0001c0001t0010 | 7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*620C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 620 | chr22 | 41674313 | |||||
chr22:41674370
|
A | C | 1 | a0001c0001t0006 | 5 | HG00733.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*563T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 563 | chr22 | 41674370 | |||||
chr22:41674512
|
A | G | 1 | a0001c0001t0007 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*421T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 421 | chr22 | 41674512 | |||||
chr22:41674625
|
C | T | 1 | a0001c0001t0009 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 308 | chr22 | 41674625 | |||||
chr22:41674789
|
C | T | 1 | a0001c0001t0002 | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*144G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 144 | chr22 | 41674789 | |||||
chr22:41674818
|
T | C | 1 | a0001c0001t0005 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*115A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 115 | chr22 | 41674818 | |||||
chr22:41674859
|
A | G | 1 | a0001c0001t0005 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 3/3 | 74 | chr22 | 41674859 | |||||
chr22:41688865
|
C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/3 | chr22 | 41688865 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41675568
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.125-373G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675568 | ||||||
chr22:41675580
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.125-385A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675580 | ||||||
chr22:41675744
|
CT | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 22 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.125-550delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675744 | ||||||
chr22:41675754
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0118 | 4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-559A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675754 | ||||||
chr22:41675826
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0060others(2): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-631A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675826 | ||||||
chr22:41675845
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0027others(11): Show | 25 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.125-650C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41675845 | ||||||
chr22:41676150
|
T | A | 1 | a0001c0001t0001g0031 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-955A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676150 | ||||||
chr22:41676152
|
T | A | 1 | a0001c0001t0001g0031 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-957A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676152 | ||||||
chr22:41676445
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.125-1250G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676445 | ||||||
chr22:41676456
|
C | A | 1 | a0001c0001t0007g0040 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.125-1261G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676456 | ||||||
chr22:41676531
|
C | CT | 16 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(13): Show | 42 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.125-1337dupA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676531 | ||||||
chr22:41676531
|
CT | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(69): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-1337delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676531 | ||||||
chr22:41676814
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1619G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676814 | ||||||
chr22:41676849
|
T | C | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-1654A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676849 | ||||||
chr22:41676908
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(99): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.125-1713G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676908 | ||||||
chr22:41676931
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.125-1736A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41676931 | ||||||
chr22:41677059
|
G | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(21): Show | 51 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.125-1864C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677059 | ||||||
chr22:41677130
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(105): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.125-1935G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677130 | ||||||
chr22:41677153
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0113 | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1958G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677153 | ||||||
chr22:41677154
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125-1959G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677154 | ||||||
chr22:41677240
|
T | C | 1 | a0001c0002t0001g0020 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.125-2045A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677240 | ||||||
chr22:41677394
|
G | A | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-2199C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677394 | ||||||
chr22:41677512
|
T | A | 1 | a0001c0001t0001g0038 | 2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.125-2317A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677512 | ||||||
chr22:41677828
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0027others(11): Show | 25 | HG01884.hp2 HG02280.hp2 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.124+2416G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677828 | ||||||
chr22:41677979
|
C | CT | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(9): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.124+2264dupA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677979 | ||||||
chr22:41677979
|
C | CTT | 3 | a0001c0001t0002g0058a0001c0001t0005g0009a0001c0001t0010g0116 | 7 | HG01175.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+2263_124+2264d others(4): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677979 | ||||||
chr22:41677998
|
C | T | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+2246G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41677998 | ||||||
chr22:41678018
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+2226G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678018 | ||||||
chr22:41678038
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.124+2206T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678038 | ||||||
chr22:41678044
|
C | T | 2 | a0001c0001t0005g0009a0001c0001t0005g0051 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+2200G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678044 | ||||||
chr22:41678124
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0092 | 3 | HG02145.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+2120G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678124 | ||||||
chr22:41678210
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(99): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.124+2034G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678210 | ||||||
chr22:41678211
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(104): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.124+2033T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678211 | ||||||
chr22:41678226
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(32): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+2018G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678226 | ||||||
chr22:41678305
|
A | G | 1 | a0001c0001t0004g0006 | 9 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1939T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678305 | ||||||
chr22:41678405
|
A | G | 1 | a0001c0001t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124+1839T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678405 | ||||||
chr22:41678474
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124+1770T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678474 | ||||||
chr22:41678591
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0068 | 6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+1653A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678591 | ||||||
chr22:41678724
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.124+1520G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678724 | ||||||
chr22:41678745
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.124+1499C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678745 | ||||||
chr22:41678770
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.124+1474T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678770 | ||||||
chr22:41678875
|
A | C | 1 | a0001c0001t0001g0011 | 5 | HG02965.hp1 HG03130.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+1369T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678875 | ||||||
chr22:41678950
|
A | T | 3 | a0001c0001t0005g0009a0001c0001t0005g0051a0001c0001t0010g0116 | 7 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1294T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41678950 | ||||||
chr22:41679079
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0055 | 2 | HG01346.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.124+1165C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679079 | ||||||
chr22:41679139
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0111 | 2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.124+1105A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679139 | ||||||
chr22:41679296
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(71): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.124+948C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679296 | ||||||
chr22:41679422
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0083 | 3 | HG00673.hp1 NA18990.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.124+822C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679422 | ||||||
chr22:41679577
|
T | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(96): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.124+667A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679577 | ||||||
chr22:41679677
|
GCT | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0030 | 4 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+565_124+566del others(2): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679677 | ||||||
chr22:41679678
|
CTT | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(104): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.124+564_124+565del others(2): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679678 | ||||||
chr22:41679996
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124+248G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41679996 | ||||||
chr22:41680159
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0081 | 2 | HG02015.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.124+85G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | 41680159 | ||||||
chr22:41680377
|
C | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(99): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.4-13G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680377 | ||||||
chr22:41680637
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(99): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.4-273T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680637 | ||||||
chr22:41680685
|
T | C | 1 | a0001c0001t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-321A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680685 | ||||||
chr22:41680858
|
C | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-494G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680858 | ||||||
chr22:41680893
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4-529G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680893 | ||||||
chr22:41680952
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(99): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.4-588G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680952 | ||||||
chr22:41680964
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-600C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680964 | ||||||
chr22:41680985
|
G | A | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-621C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41680985 | ||||||
chr22:41681104
|
G | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0101 | 2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.4-740C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681104 | ||||||
chr22:41681176
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0110 | 3 | NA18957.hp2 NA18977.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4-812T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681176 | ||||||
chr22:41681733
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.4-1369T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681733 | ||||||
chr22:41681854
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(70): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4-1490C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681854 | ||||||
chr22:41681919
|
A | T | 1 | a0001c0001t0001g0035 | 2 | NA18986.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4-1555T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681919 | ||||||
chr22:41681935
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4-1571G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681935 | ||||||
chr22:41681965
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4-1601C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681965 | ||||||
chr22:41681990
|
CT | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(102): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.4-1627delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41681990 | ||||||
chr22:41682030
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4-1666C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682030 | ||||||
chr22:41682155
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4-1791G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682155 | ||||||
chr22:41682156
|
G | A | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-1792C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682156 | ||||||
chr22:41682201
|
T | C | 1 | a0001c0001t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4-1837A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682201 | ||||||
chr22:41682359
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4-1995T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682359 | ||||||
chr22:41682449
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4-2085C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682449 | ||||||
chr22:41682453
|
G | T | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2089C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682453 | ||||||
chr22:41682509
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4-2145C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682509 | ||||||
chr22:41682662
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(71): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.4-2298T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682662 | ||||||
chr22:41682788
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0113others(1): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4-2424T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682788 | ||||||
chr22:41682800
|
C | G | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2436G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682800 | ||||||
chr22:41682805
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2441G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682805 | ||||||
chr22:41682933
|
G | A | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-2569C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41682933 | ||||||
chr22:41683008
|
T | G | 1 | a0001c0001t0002g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4-2644A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683008 | ||||||
chr22:41683012
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4-2648A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683012 | ||||||
chr22:41683030
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4-2666G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683030 | ||||||
chr22:41683042
|
C | T | 2 | a0001c0001t0005g0009a0001c0001t0005g0051 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-2678G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683042 | ||||||
chr22:41683153
|
C | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-2789G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683153 | ||||||
chr22:41683154
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-2790C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683154 | ||||||
chr22:41683162
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4-2798T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683162 | ||||||
chr22:41683235
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0068 | 6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-2871T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683235 | ||||||
chr22:41683236
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4-2872C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683236 | ||||||
chr22:41683242
|
C | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0047 | 10 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-2878G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683242 | ||||||
chr22:41683309
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4-2945G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683309 | ||||||
chr22:41683357
|
G | A | 2 | a0001c0001t0003g0014a0001c0001t0003g0053 | 4 | HG00639.hp1 HG02735.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2993C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683357 | ||||||
chr22:41683665
|
A | T | 2 | a0001c0001t0006g0093a0001c0001t0006g0094 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4-3301T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683665 | ||||||
chr22:41683728
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4-3364C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683728 | ||||||
chr22:41683730
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(70): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4-3366C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683730 | ||||||
chr22:41683900
|
T | TG | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-3537_4-3536insC | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683900 | ||||||
chr22:41683902
|
T | G | 1 | a0001c0001t0001g0016 | 3 | HG03225.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4-3538A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41683902 | ||||||
chr22:41684060
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4-3696G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684060 | ||||||
chr22:41684076
|
G | C | 2 | a0001c0002t0001g0022a0001c0002t0001g0119 | 4 | HG00408.hp2 HG00423.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-3712C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684076 | ||||||
chr22:41684184
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(97): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4-3820A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684184 | ||||||
chr22:41684266
|
G | A | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-3902C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684266 | ||||||
chr22:41684293
|
G | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(6): Show | 25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.4-3929C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684293 | ||||||
chr22:41684472
|
C | G | 1 | a0001c0001t0003g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4-4108G>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684472 | ||||||
chr22:41684528
|
T | C | 1 | a0001c0001t0001g0024 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4-4164A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684528 | ||||||
chr22:41684769
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0113others(1): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+4025C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684769 | ||||||
chr22:41684796
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+3998C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684796 | ||||||
chr22:41684799
|
T | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+3995A>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684799 | ||||||
chr22:41684926
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3+3868C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684926 | ||||||
chr22:41684951
|
T | C | 1 | a0001c0001t0001g0032 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3+3843A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684951 | ||||||
chr22:41684985
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3+3809C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41684985 | ||||||
chr22:41685059
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(71): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.3+3735C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685059 | ||||||
chr22:41685086
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3+3708G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685086 | ||||||
chr22:41685154
|
C | CA | 12 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 25 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.3+3639dupT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | ||||||
chr22:41685154
|
C | CAA | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(82): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.3+3638_3+3639dupTT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | ||||||
chr22:41685154
|
C | CAAA | 6 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0082others(3): Show | 12 | HG00597.hp2 HG01175.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+3637_3+3639dupTT others(1): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685154 | ||||||
chr22:41685246
|
G | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+3548C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685246 | ||||||
chr22:41685247
|
C | A | 1 | a0001c0001t0010g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+3547G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685247 | ||||||
chr22:41685593
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0061 | 2 | NA18942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.3+3201G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685593 | ||||||
chr22:41685599
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+3195T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685599 | ||||||
chr22:41685616
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+3178G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685616 | ||||||
chr22:41685693
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+3101A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685693 | ||||||
chr22:41685704
|
G | T | 1 | a0001c0001t0003g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3+3090C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685704 | ||||||
chr22:41685711
|
A | T | 1 | a0001c0001t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+3083T>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685711 | ||||||
chr22:41685731
|
T | C | 7 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0022others(4): Show | 17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+3063A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685731 | ||||||
chr22:41685760
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3+3034C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685760 | ||||||
chr22:41685779
|
A | G | 5 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0115others(2): Show | 13 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+3015T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685779 | ||||||
chr22:41685845
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0113 | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+2949C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685845 | ||||||
chr22:41685917
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+2877T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685917 | ||||||
chr22:41685968
|
CA | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(89): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3+2825delT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685968 | ||||||
chr22:41685968
|
CAA | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0060others(5): Show | 10 | HG01167.hp2 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+2824_3+2825delTT | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41685968 | ||||||
chr22:41686115
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+2679G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686115 | ||||||
chr22:41686127
|
G | A | 1 | a0001c0001t0008g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3+2667C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686127 | ||||||
chr22:41686155
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3+2639C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686155 | ||||||
chr22:41686243
|
T | G | 7 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0022others(4): Show | 17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+2551A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686243 | ||||||
chr22:41686304
|
CT | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0049others(7): Show | 15 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3+2489delA | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686304 | ||||||
chr22:41686325
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(36): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.3+2469C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686325 | ||||||
chr22:41686429
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0114 | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+2365G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686429 | ||||||
chr22:41686493
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+2301A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686493 | ||||||
chr22:41686497
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3+2297C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686497 | ||||||
chr22:41686712
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG01884.hp1 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3+2082G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686712 | ||||||
chr22:41686713
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3+2081C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686713 | ||||||
chr22:41686787
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(106): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3+2007A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686787 | ||||||
chr22:41686964
|
T | G | 1 | a0001c0001t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3+1830A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41686964 | ||||||
chr22:41687025
|
G | C | 1 | a0001c0001t0001g0019 | 3 | HG00099.hp1 NA20300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3+1769C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687025 | ||||||
chr22:41687041
|
C | T | 2 | a0001c0001t0005g0009a0001c0001t0005g0051 | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+1753G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687041 | ||||||
chr22:41687087
|
G | A | 4 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0119others(1): Show | 12 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1707C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687087 | ||||||
chr22:41687113
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3+1681G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687113 | ||||||
chr22:41687123
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3+1671T>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687123 | ||||||
chr22:41687161
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0113others(1): Show | 10 | HG01109.hp2 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3+1633C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687161 | ||||||
chr22:41687333
|
A | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 18 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.3+1461T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687333 | ||||||
chr22:41687403
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0045 | 6 | HG00735.hp2 HG01074.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1391G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687403 | ||||||
chr22:41687603
|
T | C | 1 | a0001c0001t0007g0040 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3+1191A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687603 | ||||||
chr22:41687762
|
T | C | 7 | a0001c0002t0001g0007a0001c0002t0001g0020a0001c0002t0001g0022others(4): Show | 17 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+1032A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687762 | ||||||
chr22:41687825
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3+969C>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687825 | ||||||
chr22:41687827
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3+967T>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687827 | ||||||
chr22:41687924
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3+870C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687924 | ||||||
chr22:41687962
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3+832C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41687962 | ||||||
chr22:41688076
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0118 | 4 | HG01109.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+718G>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688076 | ||||||
chr22:41688130
|
G | C | 1 | a0001c0001t0002g0041 | 2 | NA18979.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.3+664C>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688130 | ||||||
chr22:41688233
|
T | C | 4 | a0001c0002t0001g0007a0001c0002t0001g0022a0001c0002t0001g0119others(1): Show | 12 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+561A>G | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688233 | ||||||
chr22:41688391
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3+403C>T | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688391 | ||||||
chr22:41688478
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+316G>A | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688478 | ||||||
chr22:41688659
|
T | G | 1 | a0001c0001t0002g0122 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3+135A>C | SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | 41688659 |